Join our in experts, in a discussion driven by you, as they tackle:

In this session we'll discuss:

  • an overview of the basics of safe handling of HPAPI’s in GMP production settings
  • the traditional paradigms of engineering controls 
  • how new strategies of single-use containment can speed production process without compromising safety


Have questions you want answered?

Submit your questions in advance of this event by email sent to corie.rowe@amriglobal.com

Speakers

Brian Haney, Ph.D.

Director of Technical Operations

AMRI

Brian P. Haney received his Bachelor of Science in Chemistry from Allegheny College and his Ph.D. in Chemistry from the University of Pittsburgh. His thesis work centered on tandem radical cyclizations for the synthesis of complex natural products. Brian joined AMRI in 2000 and since 2008 has been focused on HPAPI programs.

Iain MacGilp, Ph.D.

Director, GMP Production

AMRI

Dr. Iain MacGilp is the Director of GMP Manufacturing for AMRI Glasgow. He earned his Ph.D. in Chemistry from the University of Strathclyde, Glasgow. He has been with AMRI for 14 years. Prior to that, he spent 11 years with GSK in chemical development and broader CMC development roles.

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AMRI, a global contract research and manufacturing organization, partners with the pharmaceutical and biotechnology industries to improve patient outcomes and quality of life. With locations in North America, Europe and Asia, AMRI’s team combines scientific expertise and market-leading technology to provide a complete suite of solutions in Discovery, Development, Analytical Services, API Manufacturing and Drug Product. We’ve got it down to an exact science.

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